3β,7β-dihydroxy-5α-stigmast-22-one | 434939-89-6

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 类固醇和类固醇衍生物
• 英文名称: 3β,7β-dihydroxy-5α-stigmast-22-one
• CAS: 434939-89-6
• 化学式: C₂₉H₅₀O₂
• 分子量: 430.715
• InChiKey: VLGWVZBOHNUHJF-YZFCMFISSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.85
• 重原子数：
  31.0
• 可旋转键数：
  5.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.93
• 拓扑面积：
  40.46
• 氢给体数：
  2.0
• 氢受体数：
  2.0

反应信息

• 作为反应物：
  描述：

  3β,7β-dihydroxy-5α-stigmast-22-one 在 对甲苯磺酸 、 silver carbonate 作用下， 以 甲苯 为溶剂， 生成 3,3-(ethylenedioxy)-5α-stigmast-22-en-7β-ol
  参考文献：
  名称：

  The synthesis of spermine analogs of the shark aminosterol squalamine

  摘要：

  Aminosterols isolated from the dogfish shark Squalus acanthias are promising therapeutic agents in the treatment of infection and cancer. One of these, MSI-1436, has been shown to possess antimicrobial activity slightly better than squalamine. In this study, a series of analogs of MSI-1436 have been synthesized from stigmasterol. The 7alpha-hydroxy substituent of MSI-1436 was either omitted or the stereochemistry modified to the 7beta position. Also, analogs of MSI-1436 with 24-sultate, 24-amino, and 24-hydroxy substituents were synthesized in order to assess the importance of the side chain functional group on antimicrobial activity. All of the analogs possess significant antimicrobial activity, suggesting that substitution at C7 and C24 of the aminosterols plays a minor role in their antimicrobial potency. (C) 2002 Elsevier Science Inc. All rights reserved.

  DOI：

  10.1016/s0039-128x(01)00161-1
• 作为产物：
  描述：

  7-oxostigmasterol 在 氨 、 lithium 作用下， 以 四氢呋喃 为溶剂， 反应 0.5h， 以88%的产率得到3β,7β-dihydroxy-5α-stigmast-22-one
  参考文献：
  名称：

  The synthesis of spermine analogs of the shark aminosterol squalamine

  摘要：

  Aminosterols isolated from the dogfish shark Squalus acanthias are promising therapeutic agents in the treatment of infection and cancer. One of these, MSI-1436, has been shown to possess antimicrobial activity slightly better than squalamine. In this study, a series of analogs of MSI-1436 have been synthesized from stigmasterol. The 7alpha-hydroxy substituent of MSI-1436 was either omitted or the stereochemistry modified to the 7beta position. Also, analogs of MSI-1436 with 24-sultate, 24-amino, and 24-hydroxy substituents were synthesized in order to assess the importance of the side chain functional group on antimicrobial activity. All of the analogs possess significant antimicrobial activity, suggesting that substitution at C7 and C24 of the aminosterols plays a minor role in their antimicrobial potency. (C) 2002 Elsevier Science Inc. All rights reserved.

  DOI：

  10.1016/s0039-128x(01)00161-1